chromosome breakage Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A type of chromosomal aberration characterized by an increased susceptibility to chromosomal breakage induced by treatment of cultured lymphocytes with agents such as chemical mutagens, irradiation, and alkylating agents. (Human Phenotype Ontology, HP_0003220)
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Genes

2 genes associated with the disease chromosome breakage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
XRCC1 X-ray repair complementing defective repair in Chinese hamster cells 1
XRCC3 X-ray repair complementing defective repair in Chinese hamster cells 3